Selective adsorption and photodegradation of salicylic acid by a novel magnetic molecularly imprinted mesoporous TiO2 co-doped with silver nanoparticles and carbon nanotubes (Fe3O4@mTiO2-Ag-CNTs-MIPs) under visible light
Yuan Wang , Ying Liu , Jiao Jiao , Qing-Yan Gai , Yu-Jie Fu , Run-Ze Cao
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引用次数: 0
Abstract
A novel magnetic molecularly imprinted mesoporous TiO2 co-doped with silver nanoparticles and carbon nanotubes (Fe3O4@mTiO2-Ag-CNTs-MIPs), was successfully prepared for the selective adsorption and photodegradation of salicylic acid (SA). The morphological and physicochemical properties of the prepared composite were characterized by SEM, FT-IR, XRD, VSM, UV–Vis DRS, EIS and XPS. The adsorption and photodegradation performance of Fe3O4@mTiO2-Ag-CNTs-MIPs towards SA was investigated. The results showed that Fe3O4@mTiO2-Ag-CNTs-MIPs could achieve the specific adsorption of SA with the selectivity coefficient higher than 2. Compared with Fe3O4@mTiO2, the photodegradation efficiency of Fe3O4@mTiO2-Ag-CNTs-MIPs for SA under visible light was significantly improved, indicating that the doping of CNTs and Ag together with the loading of MIPs could enhance the photocatalytic performance of the prepared composite. Under the irradiation of visible light (300 W) for 150 min, the degradation rate of SA (5 mg/L) in 50 mL of solution (pH 3) by Fe3O4@mTiO2-Ag-CNTs-MIPs (15 mg) was up to 98.41 %. Moreover, the degradation rate of the recovered Fe3O4@mTiO2-Ag-CNTs-MIPs for SA was still 87.12 % after five cycles. The primary active species for the photodegradation of SA by Fe3O4@mTiO2-Ag-CNTs-MIPs were and h+, and the potential degradation pathways of SA were elucidated by high-resolution UPLC-MS. Overall, this study constructed a promising photocatalyst Fe3O4@mTiO2-Ag-CNTs-MIPs, which was expected to effectively degrade the pollutant SA in wastewater treatment.
期刊介绍:
JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds.
All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor).
The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.